Ghana
REGULATORY AUTHORITY: Medical devices are regulated by Ghana’s FDA (Food and Drug Authority).

CLASSIFICATION SYSTEM: Devices are classified according to the EU model of risk-based classification into Classes I, IIa, IIb, III, and IV.

TIMEFRAME: The approval process takes around 3-6 months for devices for all classes.

LICENSE VALIDITY: Licenses issued in Ghana are valid for three years.

AUTHORIZED REPRESENTATIVE: An authorized representative is required.

Last updated on January 22 2015.



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For​ more information on registration in Ghana, check out the following articles on our blog:
Country at a Glance: Ghana
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